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eucaLimus

by eucatech AG 44 variants

Ref ELM30028

eucaLimus (ELM30028) is a Class III device made by eucatech AG, registered in EUDAMED on 22 May 2024 (Basic UDI-DI B-04251895600509), active as of 23 Oct 2026.

Active European Union

CE MDD

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-04251895600509 Basic UDI-DI 04251895600509UDI-DIDate22 May 2024RegisteredStatusActive

Official records

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDD Active

Specification

EUDAMED

Device name
eucaLimus Coronary Stent System with Sirolimus Drug Coating
Model / reference
ELM30028
Primary DI / UDI-DI
04251895600509
Basic UDI-DI
B-04251895600509
EMDN code
P070402010301 Coronary drug eluting stents (des) with polymers
Device class
Class III
EU registration type
Legacy device (under a directive)
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000005541

Similar devices in this category

Other devices filed under CORONARY DRUG ELUTING STENTS (DES) WITH POLYMERS.

Other devices from eucatech AG

See all devices from eucatech AG →

Properties

  • Supplied sterile
  • Implantable
  • Incorporates a medicinal substance
Other properties (9, all answered No)